Okuda A, Imagawa M, Sakai M, Muramatsu M
Department of Biochemistry, University of Tokyo Faculty of Medicine, Japan.
EMBO J. 1990 Apr;9(4):1131-5. doi: 10.1002/j.1460-2075.1990.tb08219.x.
We have recently identified an enhancer, termed GPEI, in the 5'-flanking region of the rat glutathione transferase P gene, that is composed of two imperfect TPA (phorbol 12-O-tetradecanoate 13-acetate) responsive elements (TREs). Unlike other TRE-containing enhancers, GPEI exhibits a strong transcriptional enhancing activity in F9 embryonic stem cells. Mutational analyses have revealed that the high activity of GPEI is mediated by two imperfect TREs. Each TRE-like sequence has no activity by itself but acts synergistically to form a strong enhancer which is active even in the very low level of AP-1 activity in F9 cells. Furthermore, we show that synthetic DNAs containing two perfect TREs in certain arrangements have strong transcriptional enhancing activities in F9 cells and the activity is greatly influenced by the relative orientation and the distance of two TREs.
我们最近在大鼠谷胱甘肽转移酶P基因的5'侧翼区域鉴定出一种增强子,称为GPEI,它由两个不完全的佛波醇12-O-十四烷酸酯13-乙酸酯(TPA)反应元件(TREs)组成。与其他含TRE的增强子不同,GPEI在F9胚胎干细胞中表现出很强的转录增强活性。突变分析表明,GPEI的高活性是由两个不完全的TRE介导的。每个类TRE序列本身没有活性,但协同作用形成一个强增强子,即使在F9细胞中AP-1活性水平非常低时也具有活性。此外,我们表明,以特定排列包含两个完美TRE的合成DNA在F9细胞中具有很强的转录增强活性,并且该活性受到两个TRE的相对方向和距离的极大影响。